Abstract: Schizophrenia is a highly hereditary disorder. Genetic risk is associated with a
largeKovalev, A,
Sufianov, R,
Prevedello, D,
Borba, L,
Mastronardi, L,
Ilyasova, T,
Daniel, RT,
Messerer, M,
Rassi, M,
Zhang, G (2022) of the temporal bone and divided them into three
large groups: medial, inferior, and superior—in accordance
of molecular traits. By leveraging summary statistics of published genome-wide association studies with
largeАЛЛОГЕННЫЙ БИОМАТЕРИАЛ – ИНГИБИТОР ФИБРОЗА В ИШЕМИЧЕСКИ ПОВРЕЖДЕННОМ МИОКАРДЕЛебедева, А.И.,
Гареев, Е.М.,
Афанасьев, С.А.,
Кондратьева, Д.С.,
Муслимов, С.А.,
Попов, С.В.,
Lebedeva, A.I.,
Gareev, E.M.,
Afanasiev, S.A.,
Kondratyeva, D.S.,
Muslimov, S.A.,
Popov, S.V. (2023) рубцового перерождения миокарда и выявление ключевых фиброгенных факторов (
bFGF-1, TGFb1, MMP-9), а также
Ivanova, E.,
Asadullina, D.,
Rakhimov, R.,
Izmailov, A.,
Izmailov, Al.,
Gilyazova, G.,
Galimov, Sh.,
Pavlov, V.,
Khusnutdinova, E.,
Gilyazova, I. (2022) Here we report the results of the pilot project of exosomal miRNA expression levels in clear
cellIvanova, E.,
Gilyazova, I.,
Pavlov, V.,
Izmailov, A.,
Gimalova, G.,
Karunas, A.,
Prokopenko, I.,
Khusnutdinova, E. (2022) risk of developing disease outcomes from the general population. Clear
cell renal
cell carcinoma (cc